Found: 9
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Deep cerebral venous thrombosis mimicking influenza-associated acute necrotizing encephalopathy: a case report.
- Published in:
- 2017
- By:
- Publication type:
- journal article
A Novel LRRK2 Variant p.G2294R in the WD40 Domain Identified in Familial Parkinson's Disease Affects LRRK2 Protein Levels.
- Published in:
- International Journal of Molecular Sciences, 2021, v. 22, n. 7, p. 3708, doi. 10.3390/ijms22073708
- By:
- Publication type:
- Article
Myalgia caused by chronic myositis associated with plasmacytosis: a case report.
- Published in:
- 2018
- By:
- Publication type:
- journal article
Genetic spectrum of Charcot–Marie–Tooth disease associated with myelin protein zero gene variants in Japan.
- Published in:
- Clinical Genetics, 2021, v. 99, n. 3, p. 359, doi. 10.1111/cge.13881
- By:
- Publication type:
- Article
GCH1 mutations in dopa-responsive dystonia and Parkinson’s disease.
- Published in:
- Journal of Neurology, 2018, v. 265, n. 8, p. 1860, doi. 10.1007/s00415-018-8930-8
- By:
- Publication type:
- Article
Identification of Disease-Associated Variants by Targeted Gene Panel Resequencing in Parkinson's Disease.
- Published in:
- Frontiers in Neurology, 2020, v. 11, p. N.PAG, doi. 10.3389/fneur.2020.576465
- By:
- Publication type:
- Article
COQ2 variants in Parkinson’s disease and multiple system atrophy.
- Published in:
- Journal of Neural Transmission, 2018, v. 125, n. 6, p. 937, doi. 10.1007/s00702-018-1885-1
- By:
- Publication type:
- Article
Abdominal Epilepsy Associated With Alzheimer's Disease.
- Published in:
- 2016
- By:
- Publication type:
- Letter to the Editor
Clinical heterogeneity of frontotemporal dementia and Parkinsonism linked to chromosome 17 caused by MAPT N279K mutation in relation to tau positron emission tomography features.
- Published in:
- 2019
- By:
- Publication type:
- journal article